Canonical Allele Identifier: CA2839266064

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066933_31066934insT , CM000670.2:g.31066933_31066934insT	GRCh38
NC_000008.10:g.30924449_30924450insT , CM000670.1:g.30924449_30924450insT	GRCh37
NC_000008.9:g.31043991_31043992insT	NCBI36
NG_008870.1:g.38672_38673insT , LRG_524:g.38672_38673insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-100_505-99insT MANE Select	ENSP00000298139.5:n.505-100_505-99insT
ENST00000650667.1:c.*119-100_*119-99insT	ENSP00000498593.1:n.*119-100_*119-99insT
ENST00000298139.5:c.505-100_505-99insT	ENSP00000298139.5:n.505-100_505-99insT
NM_000553.4:c.505-100_505-99insT , LRG_524t1:c.505-100_505-99insT	NP_000544.2:n.505-100_505-99insT
XM_011544639.1:c.505-100_505-99insT	XP_011542941.1:n.505-100_505-99insT
XR_949470.1:n.778-100_778-99insT
XR_949471.1:n.778-100_778-99insT
XR_949472.1:n.778-100_778-99insT
NM_000553.5:c.505-100_505-99insT	NP_000544.2:n.505-100_505-99insT
XM_011544639.3:c.505-100_505-99insT	XP_011542941.1:n.505-100_505-99insT
XM_024447265.1:c.295-100_295-99insT	XP_024303033.1:n.295-100_295-99insT
XR_949470.3:n.806-100_806-99insT
XR_949471.3:n.806-100_806-99insT
XR_949472.3:n.806-100_806-99insT
NM_000553.6:c.505-100_505-99insT MANE Select	NP_000544.2:n.505-100_505-99insT